The moderate halophile Alkalicoccus halolimnae BZ-SZ-XJ29T grows optimally in a relative broad range of 8.3% to 12.3% (wt/vol) NaCl. The draft genome consists of approximately 3.66 Mb and contains 3,534 putative genes. Various genes involved in osmotic stress were predicted, providing pertinent insights into specific adaptations to the hypersaline environment.
ABSTRACT
The moderate halophile Alkalicoccus halolimnae BZ-SZ-XJ29T grows optimally in a relative broad range of 8.3% to 12.3% (wt/vol) NaCl. The draft genome consists of approximately 3.66 Mb and contains 3,534 putative genes. Various genes involved in osmotic stress were predicted, providing pertinent insights into specific adaptations to the hypersaline environment.
ANNOUNCEMENT
The mesophilic moderately halophilic bacterium Alkalicoccus halolimnae BZ-SZ-XJ29T was aerobically isolated from a mixture of water and sediment from a salt lake in Xinjiang Uyghur Autonomous Region, China (1). Its growth occurs in the ranges of 4.3% to 24.3% (wt/vol) NaCl, pH 6.0 to 10.5, and 5°C to 41°C. To gain insight into the osmotic adaptive strategies of hypersaline stress, the draft genome of strain BZ-SZ-XJ29T was sequenced using an Illumina HiSeq 4000 platform.
Total genomic DNA (2 μg) was extracted from strain BZ-SZ-XJ29T grown under optimal conditions, as described previously (1), using a microbial DNA isolation kit (iTOP, Beijing, China) following the manufacturer’s instructions. A library for genome sequencing was constructed using the whole-genome shotgun approach with the TruSeq DNA sample preparation kit (Illumina, USA), HiSeq PE cluster kit v4-cBot (Illumina), and HiSeq 3000/4000 SBS kit (Illumina) (2, 3). Sequencing was performed with a paired-end read length of 2 × 150 bp at approximately 200× coverage. The filtered reads were quality trimmed using Quake and the Burrows-Wheeler Aligner (BWA) with the default program parameters and were de novo assembled into contigs using SOAPdenovo2 (4). A total of 5,027,473 reads with a total length of 3,668,659 bp were assembled into 59 contigs, with a GC content of 44.9% and an N50 value of 241,109 bp. Automatic annotation was performed using the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) (https://www.ncbi.nlm.nih.gov/genome/annotation_prok). Subsequently, the genome files were uploaded to the IMG-ER tool (https://img.jgi.doe.gov/cgi-bin/submit/main.cgi) for functional annotation. Among the 3,534 genes identified, 3,435 were potential protein-coding genes. Also predicted were 55 RNAs, including 4 rRNAs (2 5S RNAs, 1 16S RNA, and 1 23S RNA), 45 tRNAs, and 6 other RNAs.
Genome sequence analysis showed the presence of a number of genes encoding putative proteins potentially related to the osmotic strategies for surviving in a hypersaline environment. Identified were one gene cluster (ectA, ectB, and ectC) for ectoine biosynthesis from aspartate semialdehyde, the betA gene and betB gene for glycine betaine biosynthesis from choline, the glnA gene for l-glutamine biosynthesis from l-glutamate, the proV gene and proW gene for the glycine betaine/proline ABC transporter, the opuAC and opuBD genes for the osmoprotectant (i.e., choline, glycine betaine, and proline) transport system (ABC transporters), and the opuD gene for glycine betaine/proline transporters (betaine/carnitine/choline transporter [BCCT] family). All genes mentioned are important for maintaining osmotic balance though the “compatible solutes strategy” under high-salt conditions. Furthermore, four genes coding for Na+/solute symporters (5–8), nine genes coding for the multisubunit Na+/H+ antiporter (9, 10), and three genes coding for a monovalent cation/proton antiporter (11) were predicted. These genes might be involved in salt stress by maintaining Na+ homeostasis. Also detected were four genes (three TrkA type and one TrkH type) responsible for K+ uptake systems, implying that strain BZ-SZ-XJ29T may gain rapidly isosmotic cytoplasm though K+ as an osmolyte when coping with osmotic shock (12). As described above, many predicted genes in the genome of strain BZ-SZ-XJ29T offer valuable insights to reveal the adaptive mechanisms for maintaining osmotic balance and Na+ homeostasis under conditions of elevated salinity.
Data availability.
The draft genome sequence of Alkalicoccus halolimnae BZ-SZ-XJ29T has been deposited at GenBank under the accession number VPFE00000000. The raw sequencing reads have been submitted to the Sequence Read Archive (SRA accession number SRR9943993) and are available at NCBI under BioProject number PRJNA559242 and BioSample number SAMN12530361.
ACKNOWLEDGMENTS
This work was supported by grant 31570110 from the National Science Foundation of China (NSFC) and grants 1610042020002 and 1610042018005 from the Foundation of Graduate School of the Chinese Academy of Agricultural Sciences (CAAS).
REFERENCES
- 1.Zhao B, Lu W, Zhang S, Liu K, Yan Y, Li J. 2017. Reclassification of Bacillus saliphilus as Alkalicoccus saliphilus gen. nov., comb. nov., and description of Alkalicoccus halolimnae sp. nov., a moderately halophilic bacterium isolated from a salt lake. Int J Syst Evol Microbiol 67:1557–1563. doi: 10.1099/ijsem.0.001759. [DOI] [PubMed] [Google Scholar]
- 2.Aparicio S, Chapman J, Stupka E, Putnam N, Chia J-M, Dehal P, Christoffels A, Rash S, Hoon S, Smit A, Gelpke MDS, Roach J, Oh T, Ho IY, Wong M, Detter C, Verhoef F, Predki P, Tay A, Lucas S, Richardson P, Smith SF, Clark MS, Edwards YJK, Doggett N, Zharkikh A, Tavtigian SV, Pruss D, Barnstead M, Evans C, Baden H, Powell J, Glusman G, Rowen L, Hood L, Tan YH, Elgar G, Hawkins T, Venkatesh B, Rokhsar D, Brenner S. 2002. Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes. Science 297:1301–1310. doi: 10.1126/science.1072104. [DOI] [PubMed] [Google Scholar]
- 3.Goodwin S, McPherson JD, McCombie WR. 2016. Coming of age: ten years of next-generation sequencing technologies. Nat Rev Genet 17:333–351. doi: 10.1038/nrg.2016.49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Kelley DR, Schatz MC, Salzberg SL. 2010. Quake: quality-aware detection and correction of sequencing errors. Genome Biol 11:R116. doi: 10.1186/gb-2010-11-11-r116. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Roberts MF. 2005. Organic compatible solutes of halotolerant and halophilic microorganisms. Saline Systems 1:5. doi: 10.1186/1746-1448-1-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Kuhlmann AU, Bremer E. 2002. Osmotically regulated synthesis of the compatible solute ectoine in Bacillus pasteurii and related Bacillus spp. Appl Environ Microbiol 68:772–783. doi: 10.1128/aem.68.2.772-783.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Banciu HL, Muntyan MS. 2015. Adaptive strategies in the double-extremophilic prokaryotes inhabiting soda lakes. Curr Opin Microbiol 25:73–79. doi: 10.1016/j.mib.2015.05.003. [DOI] [PubMed] [Google Scholar]
- 8.Olkhova E, Raba M, Bracher S, Hilger D, Jung H. 2011. Homology model of the Na+/proline transporter PutP of Escherichia coli and its functional implications. J Mol Biol 406:59–74. doi: 10.1016/j.jmb.2010.11.045. [DOI] [PubMed] [Google Scholar]
- 9.Padan E, Bibi E, Ito M, Krulwich TA. 2005. Alkaline pH homeostasis in bacteria: new insights. Biochim Biophys Acta 1717:67–88. doi: 10.1016/j.bbamem.2005.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Xu N, Wang L, Cheng H, Liu Q, Liu J, Ma Y. 2016. In vitro functional characterization of the Na+/H+ antiporters in Corynebacterium glutamicum. FEMS Microbiol Lett 363:fnv237. doi: 10.1093/femsle/fnv237. [DOI] [PubMed] [Google Scholar]
- 11.Banciu HL, Sorokin DY. 2013. Adaptation in haloalkaliphiles and natronophilic bacteria, p 121–178. In Seckbach J, Oren A, Stan-Lotter H (ed), Polyextremophiles: life under multiple forms of stress. Springer, Dordrecht, The Netherlands. [Google Scholar]
- 12.Jones MK, Warner E, Oliver JD. 2008. Survival of and in situ gene expression by Vibrio vulnificus at varying salinities in estuarine environments. Appl Environ Microbiol 74:182–187. doi: 10.1128/AEM.02436-07. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The draft genome sequence of Alkalicoccus halolimnae BZ-SZ-XJ29T has been deposited at GenBank under the accession number VPFE00000000. The raw sequencing reads have been submitted to the Sequence Read Archive (SRA accession number SRR9943993) and are available at NCBI under BioProject number PRJNA559242 and BioSample number SAMN12530361.
